Canonical Allele Identifier: PA915964949
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 556487
ClinVar RCV Id: RCV000672501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Val916Phe
CA401327159
NM_001079804.3:c.2746G>T